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Active (not recruiting) Phase 3 NCT03522246

A Study in Ovarian Cancer Patients Evaluating Rucaparib and Nivolumab as Maintenance Treatment Following Response to Front-Line Platinum-Based Chemotherapy

Phase 3 – large-scale trial before approval
Conditions: Epithelial Ovarian Cancer Primary Peritoneal Fallopian Tube Cancer Newly Diagnosed FIGO Stage III-IV Partial Response Complete Response

Sponsor: pharmaand GmbH

trial.available_in: БГ
Overview
This is a Phase 3, randomized, multinational, double-blind, dual placebo-controlled, 4-arm study evaluating rucaparib and nivolumab as maintenance treatment following response to front-line treatment in newly diagnosed ovarian cancer patients. Response to treatment will be analyzed based on homologous recombination (HR) status of tumor samples.
Who can participate
Inclusion Criteria: * Newly diagnosed advanced (FIGO stage III-IV) epithelial ovarian, fallopian tube, or primary peritoneal cancer. * Completed cytoreductive surgery, including at least a bilateral salpingo-oophorectomy and partial omentectomy, either prior to chemotherapy (primary surgery) or following neoadjuvant chemotherapy (interval debulking) * Completed first-line platinum-based chemotherapy and surgery with a response, in the opinion of the Investigator * Sufficient tumor tissue for planned analysis * ECOG performance status of 0 or 1 * Patients must be 20 years of age to consent in Japan, Taiwan and South Korea; in all other participating countries patients must be 18 years of age to consent Exclusion Criteria: * Pure sarcomas or borderline tumors or mucinous tumors * Active second malignancy * Known central nervous system brain metastases * Any prior treatment for ovarian cancer, other than the first-line platinum regimen * Evidence of interstitial lung disease or active pneumonitis * Active, known or suspected autoimmune disease * Condition requiring active systemic treatment with either corticosteroids (\>10 mg daily prednisone equivalent) or other immunosuppressive medications
Locations 23
Australia (1)
Newcastle Private Hospital
New Lambton Heights , New South Wales
Belgium (1)
UZ Leven
Leuven
Canada (1)
Alberta Health Services - University of Calgary
Calgary , Alberta
Czech Republic (1)
Masaryk Memorial Cancer Institute
Brno
Denmark (1)
Aalborg University Hospital
Aalborg
Finland (1)
Kuopio University Hospital
Kuopio
Greece (1)
Attikon General University Hospital
Chaïdári , Athens
Ireland (1)
Cork University Hospital
Cork
Israel (1)
Shaare Zedek Medical Oncology
Jerusalem
Italy (1)
Centro di Riferimento Oncologico, CRO-IRCCS
Aviano
Japan (1)
University of Tsukuba Hospital
Tsukuba , Amakubo
New Zealand (1)
Auckland City Hospital
Auckland
Poland (1)
Chair & department of Obsterics, Gynaecology and Oncology (previous site)
Warsaw , Kondratowicza
Romania (1)
Spitalul Clinic Municipal "Dr. Gavril Curteanu"
Oradea , Jud. Bihor
Russia (1)
Arkhangelsk Clinical Oncological Dispensary
Arkhangelsk
Singapore (1)
National University Hospital
Singapore
South Korea (1)
National Cancer Center
Goyang-si , Gyeonggi-do
Spain (1)
Vall d'Hebron Institute of Oncology
Barcelona
Sweden (1)
Onkologiska Kliniken
Linköping
Taiwan (1)
Hualien Tzu Chi Hospital
Hualien City
Turkey (1)
Dr. Abdurrahman Yurtaslan Ankara Women's Health Education and Research Hospital
Ankara
United Kingdom (1)
East Kent Hospitals University NHS Foundation trust Medical Oncology
Canterbury , Kent
United States (1)
Arizona Oncology Associates, PC - HAL
Phoenix , Arizona
Technical details
Status
Active (not recruiting)
Phase
Phase 3
Study type
INTERVENTIONAL
Sex
Female only
Minimum age
18 Years
Healthy volunteers
No
Start date
14.05.2018
Completion date
30.12.2030
Registry ID
NCT03522246
Source
anzctr
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Information is automatically extracted from ClinicalTrials.gov. Consult your doctor before taking action.